Aspartic acid explained

Aspartic acid (symbol Asp or D;[1] the ionic form is known as aspartate), is an α-amino acid that is used in the biosynthesis of proteins.[2] The L-isomer of aspartic acid is one of the 22 proteinogenic amino acids, i.e., the building blocks of proteins. D-aspartic acid is one of two D-amino acids commonly found in mammals.[3] [4] Apart from a few rare exceptions, D-aspartic acid is not used for protein synthesis but is incorporated into some peptides and plays a role as a neurotransmitter/neuromodulator.[3]

Like all other amino acids, aspartic acid contains an amino group and a carboxylic acid. Its α-amino group is in the protonated –NH form under physiological conditions, while its α-carboxylic acid group is deprotonated −COO under physiological conditions. Aspartic acid has an acidic side chain (CH2COOH) which reacts with other amino acids, enzymes and proteins in the body. Under physiological conditions (pH 7.4) in proteins the side chain usually occurs as the negatively charged aspartate form, −COO. It is a non-essential amino acid in humans, meaning the body can synthesize it as needed. It is encoded by the codons GAU and GAC.

In proteins aspartate sidechains are often hydrogen bonded to form asx turns or asx motifs, which frequently occur at the N-termini of alpha helices.

Aspartic acid, like glutamic acid, is classified as an acidic amino acid, with a pKa of 3.9; however, in a peptide this is highly dependent on the local environment, and could be as high as 14.

The one-letter code D for aspartate was assigned arbitrarily,[5] with the proposed mnemonic asparDic acid.[6]

Discovery

Aspartic acid was first discovered in 1827 by Auguste-Arthur Plisson and Étienne Ossian Henry[7] [8] by hydrolysis of asparagine, which had been isolated from asparagus juice in 1806.[9] Their original method used lead hydroxide, but various other acids or bases are now more commonly used instead.

Forms and nomenclature

There are two forms or enantiomers of aspartic acid. The name "aspartic acid" can refer to either enantiomer or a mixture of two.[10] Of these two forms, only one, "L-aspartic acid", is directly incorporated into proteins. The biological roles of its counterpart, "D-aspartic acid" are more limited. Where enzymatic synthesis will produce one or the other, most chemical syntheses will produce both forms, "DL-aspartic acid", known as a racemic mixture.

Synthesis

Biosynthesis

In the human body, aspartate is most frequently synthesized through the transamination of oxaloacetate. The biosynthesis of aspartate is facilitated by an aminotransferase enzyme: the transfer of an amine group from another molecule such as alanine or glutamine yields aspartate and an alpha-keto acid.

Chemical synthesis

Industrially, aspartate is produced by amination of fumarate catalyzed by L-aspartate ammonia-lyase.

Racemic aspartic acid can be synthesized from diethyl sodium phthalimidomalonate,(C6H4(CO)2NC(CO2Et)2).[11]

Metabolism

In plants and microorganisms, aspartate is the precursor to several amino acids, including four that are essential for humans: methionine, threonine, isoleucine, and lysine. The conversion of aspartate to these other amino acids begins with reduction of aspartate to its "semialdehyde", O2CCH(NH2)CH2CHO. Asparagine is derived from aspartate via transamidation:

O2CCH(NH2)CH2CO2 + GC(O)NH3+ → O2CCH(NH2)CH2CONH3+ + GC(O)O(where GC(O)NH2 and GC(O)OH are glutamine and glutamic acid, respectively)

Other biochemical roles

Aspartate has many other biochemical roles. It is a metabolite in the urea cycle[12] and participates in gluconeogenesis. It carries reducing equivalents in the malate-aspartate shuttle, which utilizes the ready interconversion of aspartate and oxaloacetate, which is the oxidized (dehydrogenated) derivative of malic acid. Aspartate donates one nitrogen atom in the biosynthesis of inosine, the precursor to the purine bases. In addition, aspartic acid acts as a hydrogen acceptor in a chain of ATP synthase. Dietary L-aspartic acid has been shown to act as an inhibitor of Beta-glucuronidase, which serves to regulate enterohepatic circulation of bilirubin and bile acids.[13]

Neurotransmitter

Aspartate (the conjugate base of aspartic acid) stimulates NMDA receptors, though not as strongly as the amino acid neurotransmitter L-glutamate does.[14]

Applications & market

In 2014, the global market for aspartic acid was 39.3abbr=offNaNabbr=off[15] or about $117 million annually[16] with potential areas of growth accounting for an of $8.78 billion (Bn).[17] The three largest market segments include the U.S., Western Europe, and China. Current applications include biodegradable polymers (polyaspartic acid), low calorie sweeteners (aspartame), scale and corrosion inhibitors, and resins.

Superabsorbent polymers

One area of aspartic acid market growth is biodegradable superabsorbent polymers (SAP), and hydrogels.[18] The superabsorbent polymers market is anticipated to grow at a compound annual growth rate of 5.5% from 2014 to 2019 to reach a value of $8.78Bn globally. Around 75% of superabsorbent polymers are used in disposable diapers and an additional 20% is used for adult incontinence and feminine hygiene products. Polyaspartic acid, the polymerization product of aspartic acid, is a biodegradable substitute to polyacrylate.[19] [20] The polyaspartate market comprises a small fraction (est. < 1%) of the total SAP market.

Additional uses

In addition to SAP, aspartic acid has applications in the $19Bn fertilizer industry, where polyaspartate improves water retention and nitrogen uptake;[21] the $1.1Bn (2020) concrete floor coatings market, where polyaspartic is a low VOC, low energy alternative to traditional epoxy resins;[22] and lastly the >$5Bn scale and corrosion inhibitors market.[23]

Sources

Dietary sources

Aspartic acid is not an essential amino acid, which means that it can be synthesized from central metabolic pathway intermediates in humans, and does not need to be present in the diet. In eukaryotic cells, roughly 1 in 20 amino acids incorporated into a protein is an aspartic acid,[24] and accordingly almost any source of dietary protein will include aspartic acid. Additionally, aspartic acid is found in:

See also

External links

Notes and References

  1. Web site: Nomenclature and Symbolism for Amino Acids and Peptides . IUPAC-IUB Joint Commission on Biochemical Nomenclature . 1983 . 5 March 2018 . https://web.archive.org/web/20081009023202/http://www.chem.qmul.ac.uk/iupac/AminoAcid/AA1n2.html . 9 October 2008 . dead.
  2. Book: Fundamentals of biochemistry : life at the molecular level. G.. Voet, Judith. W.. Pratt, Charlotte. 9781118918401. 910538334. 2016-02-29. John Wiley & Sons .
  3. D'Aniello . Antimo . d-Aspartic acid: An endogenous amino acid with an important neuroendocrine role . Brain Research Reviews . 1 February 2007 . 53 . 2 . 215–234 . 10.1016/j.brainresrev.2006.08.005. 17118457 . 12709991 .
  4. Huang AS, Beigneux A, Weil ZM, Kim PM, Molliver ME, Blackshaw S, Nelson RJ, Young SG, Snyder SH . D-aspartate regulates melanocortin formation and function: behavioral alterations in D-aspartate oxidase-deficient mice . The Journal of Neuroscience . 26 . 10 . 2814–9 . March 2006 . 16525061 . 10.1523/JNEUROSCI.5060-05.2006. 6675153 .
  5. 10 July 1968 . IUPAC-IUB Commission on Biochemical Nomenclature A One-Letter Notation for Amino Acid Sequences . Journal of Biological Chemistry . en . 243 . 13 . 3557–3559 . 10.1016/S0021-9258(19)34176-6. free .
  6. Adoga . Godwin I . Nicholson . Bh . January 1988 . Letters to the editor . Biochemical Education . en . 16 . 1 . 49 . 10.1016/0307-4412(88)90026-X.
  7. Plisson . A. . Sur l'identité du malate acide d'althéine avec l'asparagine (1); et sur un acide nouveau . Journal de Pharmacie . October 1827 . 13 . 10 . 477–492 . On the identity of altheine acid malate with asparagine (1); and on a new acid . French.
  8. Book: Traité de chimie . 3 . Jöns Jakob . Berzelius . Jöns Jacob Berzelius . Olof Gustaf . Öngren . vanc . 1839 . fr . A. Wahlen et Cie.. Brussels . 81 . 25 August 2015 .
  9. Book: Plimmer, R.H.A. . R.H.A. . Plimmer . F.G. . Hopkins . vanc . The chemical composition of the proteins . January 18, 2010 . 2nd . Monographs on Biochemistry . Part I. Analysis . 1908 . 1912 . Longmans, Green and Co. . London . 112 .
  10. .
  11. .
  12. Web site: Biochemistry - Biochemistry. 2022-02-18. www.varsitytutors.com. en.
  13. Kreamer, Siegel, & Gourley. Oct 2001. A novel inhibitor of beta-glucuronidase: L-aspartic acid.. Pediatric Research. 50. 4. 460–466. 11568288. 10.1203/00006450-200110000-00007. free.
  14. Chen PE, Geballe MT, Stansfeld PJ, Johnston AR, Yuan H, Jacob AL, Snyder JP, Traynelis SF, Wyllie DJ . 13505187 . Structural features of the glutamate binding site in recombinant NR1/NR2A N-methyl-D-aspartate receptors determined by site-directed mutagenesis and molecular modeling . Molecular Pharmacology . 67 . 5 . 1470–84 . May 2005 . 15703381 . 10.1124/mol.104.008185 .
  15. Web site: Global Aspartic Acid Market By Application . Grand View Research . November 30, 2019.
  16. Book: Evans J . Commercial Amino Acids . 101–103 . BCC Research . 2014 .
  17. Transparency Market Research. Superabsorbent polymers market - global industry analysis, size, share, growth, trends and forecase, 2014-2020. (2014).
  18. Adelnia. Hossein. Blakey. Idriss. Little. Peter J.. Ta. Hang T.. 2019. Hydrogels Based on Poly(aspartic acid): Synthesis and Applications. Frontiers in Chemistry. 7. 755. English. 10.3389/fchem.2019.00755. 31799235. 2296-2646. 6861526. 2019FrCh....7..755A. free.
  19. Adelnia. Hossein. Tran. Huong D.N.. Little. Peter J.. Blakey. Idriss. Ta. Hang T.. 2021-06-14. Poly(aspartic acid) in Biomedical Applications: From Polymerization, Modification, Properties, Degradation, and Biocompatibility to Applications. ACS Biomaterials Science & Engineering. 7. 6. 2083–2105. 10.1021/acsbiomaterials.1c00150. 33797239. 10072/404497 . 232761877. free.
  20. Alford DD, Wheeler AP, Pettigrew CA . Biodegradation of thermally synthesized polyaspartate . J Environ Polym Degr . 2 . 4 . 225–236 . 1994 . 10.1007/BF02071970 . 1994JEPD....2..225A .
  21. Book: Kelling K . Crop Responses to Amisorb in the North Central Region . University of Wisconsin-Madison . 2001 .
  22. Global concrete floor coatings market will be worth US$1.1Bn by 2020. Transparency Market Research (2015).
  23. Corrosion inhibitors market analysis by product, by application, by end-use industry, and segment forecasts to 2020. Grand View Research (2014)
  24. Kozlowski LP . Proteome-pI: proteome isoelectric point database . Nucleic Acids Research . 45 . D1 . D1112–D1116 . January 2017 . 27789699 . 5210655 . 10.1093/nar/gkw978 .